The spectacle of de-extinction is often forward facing at the interface of science fiction and speculative fact, haunted by extinction’s pasts. Missing from this discourse, however, is a robust theorization of de-extinction in the present. This article presents recent developments in the emergent fields of resurrection biology and liminality to conceptualize the anabiotic (not living nor dead) state of de/extinction. Through two stories, this article explores the epistemological perturbation caused by the suspended animation of genetic material. Contrasting the genomic stories of the bucardo, a now extinct subspecies of Iberian ibex whose genome was preserved before the turn of the millennium, and the woolly mammoth, whose genome is still a work in progress, the author poses questions concerning the existential authenticity of this genomic anabiosis. They serve as archetypal illustrations of salvaged and synthesized anabiotic creatures. De/extinction is presented as a liminal state of being, both living and dead, both fact and fiction, a realm that we have growing access to through the proliferation of synthetic biology and cryopreservation. The article concludes through a presentation of anabiotic geographies, postulating on the changing biocultural significances we attach to organisms both extinct and extant, and considering their implications for the contemporary extinction crisis.
It Begins by Coming Back: The Emergence of De/extinction
Extinction is not a moment or singular event. Extinctions, as ecologically and culturally significant as they may be, are difficult to locate, define, understand, or even imagine.1 Often the term itself assumes some pre-given contextual meaning that masks its polymorphous ambiguity. Amidst narratives of Anthropocenes,2 the sixth mass extinction,3 and the emergence of novel technologies in synthetic biology,4 both conservation and geographical research face a series of epistemic and ontological questions. The multifaceted nature of extinction invites us to make sense of it empirically, in grounded and relatable “stories,”5 facilitating and affording the affective reimagining of alternatives and capacities for responses.6 Amidst an emergent ontology between existential extremes of extinct and extant, scientific speculation and practice are reworking the significances of extinction. This article aims to de-speculate biotechnical assemblages unsettling preceding epistemologies of extinction: contingent on the extinct as permanent and non-negotiable within evolutionary time. This article discusses two nonhuman protagonists at the heart of this emergent ontology: the bucardo, the only extinct animal to have ever been cloned;7 and the woolly mammoth, perhaps the most charismatic de-extinction candidate.8
The promise of de-extinction radically alters the way we perceive the event of extinction, through an introduced potential for the resurrection of extinct species. Some commentators note that it may inspire agnosticism toward extant animals,9 whereas others openly celebrate the prospect of optimism in public perceptions of conservation.10 De-extinction has been perceived by some as active engagement with the Anthropocene,11 symptomatic of the emergent role of technoscience in more-than-human relations,12 or as an extreme on the spectrum of introductory techniques in the conservationist’s toolbox.13 Many scholars in the environmental humanities have demonstrated the multiplicities of extinction.14 Through an approach inspired by this literature, this article explores the various practices and performances at the interface of biology, technology, and culture in grounding the multiplicities of de-extinction, outlining differences between the bucardo and mammoth de-extinction stories. Taking into account these multiplicities of meaning, defining de-extinction becomes increasingly difficult, especially as one comes up against questions such as: are reintroductions (say, for example, of beavers in Scotland) de-extinctions? However, for ease of argument I follow the typology of Sherkow and Greely in their 2013 Science article,15 which maintains that de-extinction comes in three forms: back-breeding, cloning, and genetic engineering.
Back-breeding, the practice of selective breeding in an attempt to reverse domestication, is an interesting approach to ecological restoration for extinct biota currently utilized by some practitioners in the rewilding movement.16 This article focuses on the cloning and genetic engineering approaches to de-extinction, due to the use of novel technologies in the genetic governance of life, and their active interactions with the genome. The bucardo and the mammoth are perhaps the classic examples for exploring the practices of speculative science in the global de-extinction discourse. Cloning as a de-extinction tool is contingent on the availability of intact genetic material.17 The bucardo is the only extinct mammal to be outlived by their cryopreserved material,18 and therefore unique in its resurrection subjection to cloning, yet in an age of salvage cryogenics it is likely the first of many. The mammoth, conversely, is de-extinction’s celebrity candidate. As elaborated by Stephanie Turner, “for extinction narratives, the development of molecular biology means that species such as woolly mammoths and Neanderthals are not lost after all, but continue to exist as genetic codes residing in their remains, codes we are getting better and better at reading and interpreting.”19 It is speculatively engaged by synthetic biologists owing to the relative abundance of its genomic material; the rate of biological deterioration diminished through the aid of permafrost. Yet intact cells remain fantastical, and as such a mammoth de-extinction would rely on a process of hybridization with the embryonic material of elephants.20
Entanglements with extinction in both of these cases are archetypal and the most developed, both theoretically and empirically, the justification for their inclusion in this essay. Beyond contrasting techniques, their juxtaposition invites reflection on the changing temporalities and materialities of extinction. Charismatic vertebrates have dominated the global de-extinction discourse, with birds and mammals populating candidate lists disproportionately.21 Invertebrates and plants are rarely featured, reflecting the broader allocation of attention in wildlife conservation. Acknowledging that drawing upon these examples may further propagate this oversight, I would emphasize that these two de-extinction stories have been selected for their technoscientific peculiarities rather than the spectacle of the animals themselves.
This article is not an argument for or against de-extinction, which is a blossoming and encapsulating debate in the ecological and environmental sciences,22 bioethics,23 law,24 genetics,25 and even tourism studies.26 The list goes on in countless other disciplines, the media, and public imaginations. Phillip Seddon speaks for a significant number of people when he affirms that “de-extinction will be pursued—the reality of the idea is too sexy to ignore, and it could be driven by aesthetic, commercial, scientific, or some other hitherto unanticipated imperatives and motivations.”27 As noted by Bill Adams, the prospect of de-extinction has the ability to grab headlines, to circulate and multiply to the extent that it has fallen out of contact with the scientific community.28 Consequentially, de-extinction has been subject to intense speculation, and the means in which many come to engage it is at the interface of science fiction and speculative fact.29 After calls for a social scientific narrative to de-speculate de-extinction,30 this article works toward a theorization of de-extinction’s geographies in the present. I begin by introducing key theoretical aspects of this changing landscape, through which to interrogate the empirical stories of the mammoth and bucardo. These changing epistemologies implicate the geographies and ontologies of extinction.
De-extinction is a speculative practice engaging the anabiotic: the liminal materiality between living and dead. Liminality is an established tradition in geography, initially conceptualized within the anthropology of ritual,31 and is commonly understood as a transitional process between and on both sides of a boundary or threshold. Examples of geographical applications have included identities in cyberspace,32 theoretical examinations of borders and diplomatic arenas,33 international relations,34 and diaspora;35 the diversity of its conceptual malleability illustrated in a recent edited book called Breaking the Boundaries: Varieties of Liminality.36 “Liminality is also a provocation to take process, creativity, and aspiration seriously.”37 Liminality is, itself, a conceptual frame that works through “shaking up epistemological assumptions”38 by collapsing binaries around constructed ontological borders, such as extinct/extant, dead/alive, immaterial/material, nonlife/life, and technological/vital. Recent scholarship has applied the concept to animals,39 or liminanimals, as Clemens Wischermann and Phillip Howell celebrate the creativity of the hybrid encounter.40 Through the stories presented later, I will explore the liminal geographies emerging at the heart of narratives encompassing taxa resurrection, those salvaged and the synthesized genomes in the geographies of de-extinction.
De-extinction technologies and ideas unsettle, distort, and disfigure the spaces and temporalities of extinction. This liminal state of de/extinction recalibrates genetics and the genome into a multifaceted existence, being both in potentiality as information and in actuality as deoxyribonucleic acids, exceeding and encompassing the aforementioned dualisms. I use a slash (/) to differentiate this existential liminality from the concept or process of resurrecting extinct taxa that is denoted by hyphenation (-). This discursive function of the slash indicates “an active and reiterative (intra-active) rethinking of the binary,”41 allowing the conceptualization of binaries as dynamic and enmeshed rather than strictly oppositional,42 as liminal and uncanny. Depending on context, a slash can be used in three ways: to denote “and,” “or,” or the spanning of two discrete categories (e.g. 2011/12). De/extinction should be thought of as a proactive and interactive questioning of the extinction concept, one accounting for both extinction and de-extinction as coexisting actions perpetually rethinking one another, forceful and metamorphic. De/extinction is relative and only makes sense with a contemplation of trace; that is, to consider de-extinction is to consider what extinction is not, and vice-versa.43 This ontology exists in a plane of potentiality with agency to shape the ways we engage with and perceive the worlds we inhabit, certainly questioning the notion of extinctions as irreversible and indefinite.
In what follows this article will explore liminal materialities, two anabiotic existences that unsettle the previously held epistemologies of extinct and extant: the bucardo and the mammoth. Through exploring the materialities and agencies of DNA itself, these genomes distort the discreteness of life and death. Biologists engaging de/extinction optimistically make sense of candidate genomes dissimilarly: they are the salvaged ghosts of extinction’s lost pasts, the synthesized ghosts of extinction’s lost futures. The bucardo and the mammoth provide archetypal illustrations of salvaged and synthesized anabiosis, the “not anymore” and “not there yet.” Genomes are simultaneously material amino acids and immaterial codes of semiotic programming, the program of which is referred to as a text by the molecular biologist, the scriptural model of which Derrida contends is central to advances in postwar science.44 “Literary metaphors have been woven into the fabric of molecular biology since its inception. The determination of the human genome sequence has brought these metaphors to the forefront of the popular imagination, with the natural extension of the notion of DNA as language to that of the genome as the ‘book of life.’”45 These systems of meaning are appropriately engaged through a posthumanist lens, which “expresses multiple ecologies of belonging,”46 encompassing the matters of language, discourse, culture; but, most notably, matter itself. Posthumanist thought has been influenced through Derrida’s writings on biology, founded through his conceptualization of trace [trace],47 referring to that which formulates difference and its deferral of meaning [différance].48 This postponement of action or event creates meaning and presence through absence, and is the opening in which binary oppositions can operate: those aforementioned concepts of life/death, extant/extinct, and nature/culture. Exploring the trace of bucardo and mammoth’s genomes poses to offer insights into what anabiosis ontologically and existentially is at present.
Salvaged Anabiosis: Bucardo
For the first and only time in history a mammal has been outlasted by its own living cells . . . welcome to anabiosis. The bucardo (Capra pyrenaica pyrenaica) has always been a spectral animal, owing its fame to a liminal presence/absence, desired—but rarely encountered—by the bourgeois hunters whom it would attract to the Pyrenees from Victorian England.49 As a magnificent and impressionable animal, the bucardo became renowned as the most sought-after trophy among the European upper classes, as its image and legend circulated throughout Europe in the late-nineteenth century (fig. 1). Officially, the bucardo has been recognized as a subspecies of Iberian ibex (or wild goat), a status unchanged since the influential publications of Ángel Cabrera in 1911.50 To avoid opening a Pandora’s box of taxonomic debate, it is crucial to note that these classifications have been greatly contested since the emergence of genetic knowledges,51 and that there exists varied schools of thought regarding the bucardo’s status as a species, subspecies, or race of ibex.52 Subject to numerous cave-art depictions in both Marsoulas and Lascaux, the bucardo arrived in the Pyrenees circa 90,000 years ago during the Palaeolithic period and thrived.53
Their habitat had spanned from the Atlantic to the Mediterranean, however by 1907 the bucardo population had been reduced to a small nucleus of eight or nine individuals, described by Cabrera as refugees (refugiados) scattered throughout the secluded valleys of Mount Perdido, in the high altitudes of Aragón, Spain.54 The lack of ecological concern regarding the diminution of the bucardo population was largely due to its almost less entitled status as a subspecies,55 which even today in the eyes of many conservation organizations equates to less importance in terms of biodiversity conservation. Together with a lack of habitat protection and increased human presence in the Pyrenees, centuries of overhunting had reduced the bucardo to an existence on the edge of extinction. However, the cultural status of the elusive animal played a significant role in the formation of one of Spain’s oldest national parks in 1918, Ordesa y Monte Perdido.56 Due to both the sheer infrequency of bucardo sightings and the dooming legacy of war, population estimates were uncommon and always highly uncertain.57 By the 1990s there were between six and fourteen individuals,58 and in 1997 there remained just one female left, known to many internationally as Celia.59
De/extinction is an ontological category that speaks to the anabiotic. Anabiosis, coming from the Greek ana- (ἀνά: again, anew) and -biosis (βίωσις: a specified mode of vital existence), is an out-of-fashion term in biology and medicine that signifies a return to life from a seemingly dead organism.60 The introduction of anabiosis was firmly rooted in Enlightenment thought, inspired by the eighteenth-century experiments and philosophies of John Hunter and Benjamin Franklin, who sought to prolong life though a primitive form of cryogenics.61 The concept was of biological intrigue for some time, including an 1860 commission by the Société de Biologie in Paris62 and revisited by Russian and Soviet scientists in the early twentieth century.63 In the context of this article, anabiosis can be thought of as the liminal realm between life and nonlife, a spatiotemporal interruption of extinction or death mediated through emergent technoscientific assemblages. Under present scientific capabilities, anabiosis is found through two scientific approaches: cloning from cryogenics and genetic engineering. Both of these approaches pose questions concerning the authenticity of de-extinction due to a range of ecological and genetic issues;64 for instance, “Is a bucardo clone born in a laboratory a genuine de-extinction?” “Is a genetically engineered elephant that genetically and morphologically resembles a mammoth really a mammoth?” The significance and exceptionality of de-extinction as a practice is its entanglement and interactivity with “the discontinuity or breakdown of some molecular, cellular, behavioural, and ecological processes,”65 a radical rethinking of this discontinuity, or an experiment with the anabiotic.
The last bucardo died as she was crushed under a falling fir tree on the sixth of January 2000. But this was no ordinary death. It was the genesis of new meanings within the technoscientific assemblages mediating, engaging, and understanding what death is. This was an extinction preceded by salvage genomics. Less than a year before her death, in a final attempt to preserve the bucardo’s genetic resources, Celia was captured, and cells from a skin biopsy were obtained, multiplied, and kept frozen in liquid nitrogen.66 Such practice would never have materialized without the imaginings facilitated by the fascinations of both science and the media with the world’s most famous lamb, Dolly, born only a few years earlier. Comparable and not disassociated with the contemporary epistemological tremors radiating from de/extinction, Dolly’s birth in 1996 changed reproductive biology forever through a biocultural reframing of the possible, as an assemblage choreographed through reproductive technologies facilitated the coming together of divergent ontologies.67 As sociologist Sarah Franklin elaborates, it is unviable to separate Dolly’s creation from the hype that surrounds it, “insofar as hype refers to imagined sets of connections and exaggerated implications, it signifies a reaching beyond, or an expansion of range. Dolly is in this sense both a frontier and a horizon—a relational someplace and no place signalling future possibility and direction.”68 Dolly’s hype is therefore her unique concurrent platforming as a figurative technological frontier and the literal embodiment of nuclear transfer. As Franklin argues, the resultant phenomenon of Dollymania cannot be reduced to fallaciousness; it is this very hype which makes her charisma as an iconic and symbolic animal of great sociocultural significance. A technoscientific floodgate had been opened, and cloning techniques were all at once reframed within our conceptualizations of what is possible.
Dollymania had merged science fiction with speculative fact, and a team from the animal reproduction laboratory at the Centro de Investigación Tecnología y Agroalimentaria of Aragón were seeing the diminution of the bucardo population to just one female under a new lens of opportunity, outside scientific normativity. Even before the successful skin biopsy on Celia, a 1998 piece in La Vanguardia discussed the possibility of her cloning,69 as most media and popular science discourses following the 1999 capture-release drew technical parallels between Celia and Dolly as stories of genetic research and technological advancement.70 This is what contextualizes Celia’s story and makes apparent the sheer partialities of de/extinction; the genealogy which transformed her genes from that of a wild thing into a space of experimentation as an animal of potentiality understood in terms of an orientation toward the future.71 The bucardo had to be imagined as anabiotic, its materiality becoming one with an entirely altered and radically different biocultural coding.
Once the skin biopsy had been performed, Celia’s cells were transported to a laboratory in the outskirts of Zaragoza, where they began to take on new meanings; her genes themselves entangled in a meshwork of contrasting ontologies facilitated by genetic and cryogenic technologies. In fact, this material and geographical disjunction (of living cells and living animal) facilitated an unprecedented response to the death of the last bucardo, who died just a few months later having been re-released to her habitat in Ordesa. Of course, many grieved and mourned the loss of an iconic animal who had become profoundly interwoven into the cultural landscape of the Pyrenees, yet like extinctions of most charismatic fauna the absence of hope was by now deeply entrenched. The bucardo had been considered essentially extinct long before Celia’s death, and for over a century it had simply been as if the inevitable were being delayed. Somatic cell nuclear transfer and the emergence of reproductive cloning had given new life to the bucardo, albeit solely through potentiality, because there existed some fleeting idea that the process might one day repopulate the Pyrenees.72 Laboratories are peculiar sites of knowledge production, where the coming together of experiences and expertise takes place on interpersonal levels, and the scientists in Zaragoza collaborated with a group of French cell biologists who had in 1998 successfully completed nuclear transfer from skin biopsies.73 Bucardo nuclei were transferred into denucleated oocytes collected from various goat and ibex females, a method which had been practiced by the Aragonese team some years before,74 all the time working with the intention of constructing a strategy of bucardo cloning.75
The donors of these oocytes—immature egg cells produced by female mammals through the process of oogenesis—were curious mixtures of Capra hybrids who lived and grazed in the fields outside the laboratory where Celia’s cells were enmeshed in a multiplicity of epistemological processes.76 These hybrids of Spanish ibex (C. pyrenaica hispanica) and domestic goats (C. hircus) were interspecies liminanimals, themselves created for the purposes of surrogacy, animals with the conceivability of carrying a bucardo clone at the interface of feral/cultivated/wild.77 The gestation period of the Spanish ibex is closer to that of the bucardo, meaning a fetus would have sufficient time for development. Despite this, they are unable to maintain prenatal health in captivity; domestic goats, on the other hand, are able to bear kids in captivity, however their shorter gestation period would likely result in the underdevelopment of a bucardo clone.
In her book Transpositions, posthumanist philosopher Rosi Braidotti defines the genetic social imaginary,78 whereby a perception of the genome as a data bank of potentiality has constructed certain cultural ideas about bodies and their function. Similarly, the emergence of anabiotic imaginaries through the development of both ideas and technologies within the bioscientific remits of de/extinction have engendered new societal approaches to agencies of the genetic in more-than-human worlds. A medley of hybridities—surrogate Capras, bucardo nuclei, and denucleated oocytes—all facilitated by a technoscientific assemblage of practical apparatus and knowledges resulted in the production of fifty-seven bucardo embryos.79 Following embryonic transfer, an animal had been impregnated by a ghost for the only occasion in history, and the time was well and truly out of joint.
“It was Wednesday, July 30, 2003, a turning point in the history of biology. For on that date, all at once, extinction was no longer forever,” proclaimed the synthetic biologist George Church in his coauthored book Regenesis: How Synthetic Biology Will Reinvent Nature and Ourselves.80 Seven years after the first mammal birth following somatic cell nuclear transfer, geneticists had, even for seven minutes alone, defied biology’s most inevitable certainty. As discussed in the article detailing the practice of the bucardo clone:
The delivered kid was genetically identical to the bucardo, disregarding the influences of mitochondrial DNA from the oocyte of the domestic donor and of the uterine environment of the hybrid recipient. The newborn displayed serious respiratory distress and died [a] few minutes after the caesarean section. . . . At present it can be assumed that cloning is a not very effective way to preserve endangered species, because the complexity to handling the experimental wild animal and the insufficient knowledge on both, the cellular mechanisms involved in the technique and on the reproductive characteristics of the animals. . . . However, in species as bucardo, cloning is the only possibility to avoid its complete disappearance. The present work encourages [conservationists] to appropriately store somatic tissues and cells of all endangered species or suitable animals, as they may be useful for future cloning-based conservation programs.81
Whether this was a genuine de-extinction or not depends on who you ask: for the likes of George Church and other high-profile supporters of de-extinction, this was a greatly significant event that signaled the end of extinction as we knew it. For critics of the global de-extinction movement this was a failed cloning attempt that, even had the clone lived and experienced life beyond the walls of a laboratory, would have amounted to nothing more than the clone of an “old, infertile, highly heterozygous female”—a singular specimen further prolonging the inevitability of bucardo extinction.82 Regardless of opinion, this exemplifies the liminal ambiguity of de/extinction, at once the archetypal case of reversing extinction, while at the same time the clone of an animal from anabiotic cells that had never been extinct; after all, “it made no difference to the frozen cells that they happened to be last of the line: cells were cells.”83 Engaging the geography and political ecology of these cells, too, would maintain that they are materially inseparable from their entanglement in processes of ongoing habitat degradation and commodification. The mere eventuality in which a species is outlived by its genomic materiality is one that is open to a plethora of critical scholarship.84
De/extinction is a haunting, or in Jacques Derrida’s terms,85 a hauntology (hantologie): it simultaneously speaks to and from both absence and presence. This hauntology is a geographical rupture through the figure of the ghost, itself neither living or dead, neither absent nor present. Derrida writes
Repetition and first time: this is perhaps the question of the event of the ghost. What is a ghost? What is the effectivity or the presence of a specter, that is, of what seems to remain as ineffective, virtual, insubstantial as a simulacrum? Is there there, between the thing itself and its simulacrum, an opposition that holds up? Repetition and first time, but also repetitions and last time, since the singularity of any first time, makes it also a last time. Altogether other. Staging for the end of history. Let us call it a hauntology . . . a question of repetition: a specter is always a revenant. One cannot control its comings and goings because it begins by coming back. . . . What seems almost impossible is to speak always of the specter, to speak to the specter, to speak with it, therefore especially to make or to let a spirit speak.86
Ghosts have become of interest recently within the humanities of wildlife and conservation,87 particularly as the forceful and affective capacities of hauntings are understood in terms of their potential to inspire novel modes of environmentalism, as these “ghosts remind us that we live in an impossible present—a time of rupture, a world haunted by the threat of extinction.”88 This hauntology of de/extinction is never present or absent, it is always both, speaking to, with, and of the living and the dead; or rather, actively challenging and passing between the boundaries that make these categories distinct, beginning by coming back.
The event of the bucardo’s cloning shook the authority of extinction. But it also brought into question the authority of de-extinction as an anabiotic imaginary: how would other animals, such as the thylacine or passenger pigeon, ever become revenants if we were unable to reverse extinction with living cells? To this day, it highlights the subjective and multiple meanings of de/extinction and the spectrality of nonhuman existence in the post-genomic age, speaking to a conjuring, a revenant, in which “the living maintain the dead, play dead, let themselves be entertained and occupied and played or tricked [jouer] by the dead, speak them and speak to them.”89 It signaled a possibility, further plunging into the metaphysical arena of haunting: both present and absent, living and dead, fact and fiction.
Playing himself in Ken McMullen’s experimental film Ghost Dance,90 Derrida argues that rather than distancing us from the realm of ghosts, modern technologies enhance the power of ghosts to haunt us. The bucardo’s cells are still kept in two locations, living, but also dead. It was not only the first de-extinct animal but also the first to go extinct twice, subject to what we could call a re-extinction. It is the only example of a mammal whose cells have outlived its population, who is anabiotically entangled in the liminal geographies of de/extinction, distorted between the spaces of science and evolution. Synthetic biologists look to the story of the bucardo as one of inspiration, as the dawn of the de-extinction age, and these events are revisited every day in laboratories around the world through the anabiotic imaginaries of other charismatic fauna defying our previously held ontologies of extinction.
Synthesized Anabiosis: Mammoth
Technically and methodologically, the events punctuating the cloning of the bucardo were almost identical to that of Dolly, albeit this time mediated through interspecific somatic cell transfer as opposed to within the same species (a feat achieved just once before with the cloning of the gaur—the Indian bison—whose clone had also died shortly after birth, further highlighting the technological difficulties of this process).91 For animals such as the bucardo, their anabiosis is imagined and engaged as an idea, while there are still populations living. This is evident through the precautionary cryogenic measures gaining popularity among many conservationists, those intent on “freezing the ark,”92 an act which itself defies the distinctions of life/nonlife and living/nonliving.93 Yet just as “Dollymania” profoundly affected the significance of the bucardo’s de/extinction, anabiotic imaginaries of species lost far before living memory are emerging in laboratories all over the world due to advances in DNA sequencing and synthesis. How may we begin to engage with the idea of animals long-gone being-here?
The woolly mammoth (Mammuthus primigenius) was depicted alongside ibex some 15,000 years ago in the caves of the Pyrenees (fig. 2).94 It is the most famous extinct mammal and had suffered extinction long before humans learned to inscribe language. Contemporary imaginaries of mammoths are the product of strange biocultural assemblages. At the interface of cave art we are encouraged to experience the elemental differences of non/inhuman forces, suggesting “an ontological intimacy with other entities and the dismantling of the boundaries between life and environment.”95 Cave art is inseparable from engagements with deep time: the geologic and the genetic. The traces of biological remains left by the mammoth, scattered through the Siberian tundra, offer these potentials of multitemporal affective encounters. If we understand these genomic traces in the Derridean sense, then they function as ontological and epistemological opportunities for the questioning of boundaries, like those of extinct and extant. To engage and perform the revenants of deep time, speculative experimentation is utilized using a range of rapidly developing technologies. Living cells are required to perform somatic cell transfer, and therefore the anabiosis of animals long-gone must materialize in another manner, through anabiotic synthesis.
Synthesizing the Anabiotic
The mammoth is engaged through another anabiotic approach, one further virtualized from the material world but just as real. Information is the lowest common denominator of all genetics, and since the sequencing of the human genome in 2003 a plethora of opportunities have emerged facilitating a greater understanding of ancient DNA and a technological capacity to assemble the genomes of extinct taxa.96 Beth Shapiro, evolutionary molecular biologist, and the author of How to Clone a Mammoth,97 has routinely maintained that the coinciding of these techno-epistemological developments pave “the most likely route to de-extinction . . . advances in ancient DNA (aDNA) extraction and DNA sequencing technologies are making it increasingly feasible to reconstruct full genome sequences from extinct species.”98 In conjunction with long cultural fascinations surrounding the charismatic megafauna, often spurred by the excitement surrounding the discovery of remains (of either bodies or ancient depictions), genome sequencing has afforded novel systems of allowing the mammoth specters to speak and affect us. aDNA understandings and practices have developed at a staggering rate over the past decades; the materiality of mammoth genome being translated into coded information through quantitative polymerase chain reaction sequencing comparatively using both Asian and African elephant genomes.99 Sequence identity between mammoth aDNA and African elephant DNA has been found to be greater than 98.5 percent,100 meaning that most mammoth DNA is among living animals today.
All biological life is a living library of aDNA enmeshed deeply within evolutionary time. For the synthetic biologist, amidst the technoscientific possibilities of cutting and pasting genomes as if assembled on a Microsoft Word document, these hybridities-to-come will depend on the “genomes of living species [that] must be used as scaffolds to align ancient DNA fragments.”101 This synthesis of life is not devoid of human intervention, as is endemic in questions of liminality between humans and other animals.102 These uncanny beings would have a unprecedented genetic makeup: the evolutionary time would be out of joint. As described by Beth Shapiro,
Coincident with the release of the latest in the Jurassic Park series of movies, George Church’s lab at Harvard University’s Wyss Institute reported their first successes in editing living elephant cells so that they contain gene sequences from the elephant’s recently extinct relative, the woolly mammoth. Using a CRISPR (clustered regularly interspaced short palindromic repeats)-Cas9 approach, Church’s team replaced 14 loci in the elephant genome with the mammoth version of those sequences. Although they have not yet created a mammoth, their success blurred the already fuzzy line that separates science from science fiction, bolstering hopes (and fears) that de-extinction, the resurrection of extinct species, may soon be reality.103
Bill Adams has noted that synthetic biology is just seen by many conservationists as one extreme of new methodologies and epistemologies centered on tweaking genomes in wildlife conservation.104 Others have considered the potential for functional de-extinction within biological epistemological frameworks founded on the ecological species concept, whereby the niche receives definitional priority over the genetic code, affording the ability of nonhuman self-definition through action and interaction.105 This identification is therefore one guided by animals’ geographies,106 whereby the lived ecologies, habitats, and trophic function are understood as the raison d’être, not only evolutionary histories.
Anabiotic synthesis is an engagement with biological time machines,107 where “at a minimum, the choice of a species concept is ambiguous with respect to the definition of ‘extinction.’”108 The perception of taxa as self-defined through their own agencies and ecological exchanges expresses an affinity for hauntology and de/extinction, as made apparent by many ideas among rewilding practitioners working with the proxies of animals long gone such as the auroch109—the ancestor of domestic cattle—the idea of which has been spectacularized by molecular biologists and the development of synthetic biology. Genetically, these anabiotic syntheses are challenging previously held categorizations at the species-level; the chimera that could be born as a result of this genomic engineering would be a mammoth based on function rather than (genetic) form, realized through hybridization.
George Church discusses potential hybridizations with extinct species as exciting new dawns for life on Earth, as he outlines to a crowded room at the internationally renowned TEDx DeExtinction event: “We’re trying to make species from information alone.”110 Interestingly, this event projects de/extinction as ageographical in the scientific sense, whereby the methods, theories, and practices of de-extinction are bestowed as universal. However, exploring the empirical diversity of the event itself, which utilizes a range of nonhuman protagonists, technological practices, and imaginaries of future environmentalism, illustrates rather explicitly the importance of geographies in de/extinction (for example those considerations of habitat, history, cultural and ecological significance). A synthesis of the anabiotic, founded through the engagement of genetics as information and code, has given new life to the mammoth through potentiality and speculation. The permanence of extinction is called into question through genomic hybridization and the emergence of genetic liminalities. Just as endangered taxa are seen through a different lens in an era of cryogenic conservation and the development of interspecific cell transfer technologies, animals (and plants) that have been absent from Earth for a considerable time are given new presence through the concept of anabiotic synthesis.
De/extinction and Potentiality
If we revisit anthropological ideas of potentiality, one could make a case that the mammoth could already be classed as de/extinct, as are many taxa disturbing the finality of extinction. The post-genomic era is one that has been marked by the discourses of potentiality, often articulated as a “hopeful idiom through which to imagine,”111 a virtuality with its own reality and cultural agency. Revive and Restore, a foundation and advocacy organization that has secured considerable funding for de-extinction projects in the United States, portrays its mammoth project in a comparable vein of potentiality:
As the possibilities of biotechnology innovations were revealed, the idea of resurrecting the woolly mammoth quickly captured the imagination. . . . Breakthrough advances in genomic biotechnology are presenting the possibility of bringing back long-extinct species—or at least proxy species with traits and ecological functions similar to the extinct originals. . . . Not only does this research build the foundations of mammoth de-extinction, it provides potentially valuable insight to evolution for different climate conditions. . . . Dr. Zimov’s perspective illuminates an additional function that must be considered: the mammoth’s potential role in providing resilience in the face of climate change. . . . Mammoth haemoglobin, for example, may reveal information about mammalian blood useful to treating human diseases, and potentially the future of human space exploration.112
The mammoth is already engaged in multiple meanings, subject to potentialization as a symbolic project, already guiding scientific and technological innovations of the future. Its resurrection is discussed by de/extinction practitioners with an air of certainty and inevitability, allowing cultural imaginaries to develop as the virtual is interwoven into ideas of wildlife and extinction. The mammoth is currently actualized in narratives of research and epistemological function; as a means of developing scientific understandings of ecological niches, (paleo)climatology, climate change resilience, human health and epidemiology, and even the prospects of space exploration and terraforming. Such becomings profoundly question the idea of the mammoth as an extinct animal. These anabiotic imaginaries are very much real, and cultural responses from both inside and outside the scientific community animate the mammoth as an animal of the future, while simultaneously an animal of the past.
It is a haunting, a question of repetition and first time, a return to as a departure from. It is already present in its absence, and absent in its presence. Consider the well-known case of Sergey Zimov’s Pleistocene Park in Siberia,113 “the future of the past,” where the mammoth is the affective and charismatic driving force for the (re)establishment of an ecosystem that resembles the most recent glacial maximum. This radical attempt to engage wildlife is inseparable from the ghosts of mammoths and is just one example of how the fauna is defying the idea of a simple categorization between extinct and extant: the mammoth is already the pioneer of conservation projects and a contributor to knowledge production in conservation biology. It is de/extinct through its potentiality, its genomic liminality enacting material changes all over the world, a life of virtual reality.
These two very different de/extinction accounts have illustrated the changing natures of extinction in the post-genomic age. According to McCauley et al., “Historically, extinction was permanent in a way that few biological processes are. The binary finality of extinction, however, is being challenged by fast-moving progress in de-extinction science.”114 Genomes themselves have emerged as the material and immaterial subjects of novel ideas about how humans and nonhumans engage and affect one another. They are subjugated and made sense of through human and technological modes of signification yet oblivious to these meanings;115 simultaneously as the actual living thing in the test tube, and/or as the virtual nonliving thing signified as a potentiality through genetic code, acting in between. I agree with de/extinction scientist Ben Novak when he states that “biotechnology changes the concept of extinction,”116 yet I would contend that these biotechnologies are produced at the interface of wildlife, endangerment, and extinction being subjected to the future imaginaries of resurrection. In an era of hauntings.
Of first times and repetitions. Cells extracted from bucardo skin in the last millennium continue existing in their anabiotic state in vitro, their cloning viability unaltered, as recently confirmed by a scoping study in 2013.117 “The bucardo population consists of zero multi-celled individuals and several million single-celled clonal individuals currently cryopreserved.”118 And the mammoth genome exists as information and through the labor of synthetic biology, the result of countless genetic studies and experiments, as signifier of potentiality. But their effects are felt by living things making sense of the world, with real politics and real geographies. From the perspective of scientific practice, there is some concern that this is a somewhat tunnel-vision approach that aims to “mimic the biology of extinct species, but fails to resurrect their ecology.”119 It is essential that the de/extinction is contextualized and ecologized, within trophic entanglements as well as cultural landscapes.
The liminality of de/extinction in the present is taking-place and taking-shape in numerous contexts as a genomic library of nonhuman life; while technologies and imaginaries emerge so too are conceptualizations of immortality at the population level. The epistemological conventions of extinction are just as relevant, albeit with changed significances, and conservation will need to grapple with the possibility of a conservation without extinction in response. What might that mean, and how might that materialize? Perhaps living within anabiotic worlds may inspire apathy toward the diversity of wildlife on Earth. If extinction isn’t a permanent deal, why devote our attention and resources to the protection of nonhuman life when it could go elsewhere? It even may engender hyper-conservative and promethean narratives akin to that of ecomodernism, whereby global ecocide may be tolerated in the present due to a conviction that there will be a technological fix somewhere in the future. Such horizons are disquieting but may be mitigated or evaded through robust narratives from the social sciences and humanities of wildlife conservation, where de/extinction should be an invitation to consider wildlife beyond the simple binary quantification of dead or alive, extinct or extant. Whether opposed to or in favor of the concept of technologically (re?)introducing ghosts into ecosystems, this liminal category may feasibly serve as a stimulus to uncover new affective connections with living things, attending to recombinant and subjective ecologies.
The liminal geographies of de/extinction are intriguing and complex. They are opportunities for creativity and new epistemologies. This betwixt and between area, between being extinct and being extant, is profoundly geographical and multiple, deeply entangled within the politics and histories of relationships between living organisms, their environments, and their ecologies. Extinctions and de-extinctions take place and are materialized through some application of cultural and ecological significance, which tends to favor charismatic and spectacular nonhumans. In these emerging geographies encompassing the anabiotic, we find novel circumstances and chances for a rethinking of the role of humans and technologies in the diversity of worldly life. The salvaged and the synthesized creatures of scientific work emerge as compelling and uncanny mediators.
Earth is home to an innumerable magnitude of virtually extinct taxa, examples where it is merely a matter of time before the last individual passes away. And as anabiotic geographies emerge in many of these contexts, the lives and actions of those who remain are enmeshed within imaginaries regarding their resurrection, as recently exemplified by the discourses surrounding the northern white rhino. Extinction is an incredibly useful concept that makes conservation decision-making significantly easier. However perhaps it is time to embrace radically different objectives in the ways we relate with and to wildlife, such as those prioritizing the agencies and geographies of nonhumans, as the ontological foundations for the global rewilding movement have sought to engage. Many new modes of understanding have explored these cosmopolitics for wildlife, which are “not neatly aligned, linear, or concordant.”120 And in many cases, as illustrated through countless accounts of science fiction (think the Jurassic Park enterprise), the futures of de/extinction may seem like a disaster. But similar to Jamie Lorimer’s take on the Anthropocene, with this comes the presentation of novel opportunities for understanding existence on Earth.
These anabiotic geographies are very much real and a key element of our relationship with nonhuman life, and as technological and cultural capacities for engaging these worlds develop, agencies of the anabiotic will become an even greater aspect of these encounters. But, as I hope these de/extinction stories have illustrated, de/extinction is not just an inevitability of the future. It is active and forceful in the present, entangled in geographies and histories of extinctions and endangerments worldwide, speaking to specters and allowing them to speak to us.
I would like to thank Bill Adams and Jonny Turnbull for countless hours of conversation that have undoubtedly found their way into this article and for comments on earlier versions of this article that were presented at the Unviersidade de Santiago de Compostela in September 2018 during the inaugural “Rethinking Animality” conference and at the conference “Animal Remains,” which was held at the University of Sheffield in April 2019. Many thanks to Ben Garlick and Kate Symons for their work on this exciting special issue and to Thom van Dooren for assistance in the editorial process.
Wischermann and Howell, “Liminality.”
Cabrera, “The Subspecies of the Spanish Ibex” and Fauna Iberica.
The name Celia was popularized within the Anglophone press and is how the last bucardo became known internationally; however, it is important to note that those from the settlement of Torla-Ordesa (which has an incredibly rich history of human-bucardo interactions) know her as Laña. For purpose of narrative, I refer to her as Celia, as this is how she was named and perceived by the geneticists whose thought and worldviews made the bucardo’s de/extinction spectacular.
“Anabiosis,” Oxford English Dictionary.
For a discussion of de-extinction’s authenticity, see Siipi, “The Authenticity of Animals.”
For a thorough and stimulating discussion, see Thompson, Making Parents.
This threefold classification is a key theme of Maan Barua’s Urban Ecologies research Project (http://urbanecologies.org/).
Church and Regis, Regenesis, 134.
For a comprehensive and radical take on extinction, see Moore, Capitalism in the Web of Life.
I borrow this term from Loi et al., “Biological Time Machines.”
A theme explored in the context of microbial life by Paxson and Helmreich, “Microbial Abundance.”